broadinstitute / gnomad-browser
Explore gnomAD datasets on the web
☆81Updated this week
Related projects: ⓘ
- ☆65Updated last week
- Hail helper functions for the gnomAD project and Translational Genomics Group☆86Updated this week
- Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF☆138Updated 4 months ago
- Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls☆187Updated 3 years ago
- Browser for ExAC consortium data☆106Updated 2 years ago
- IGV Web App☆114Updated 2 weeks ago
- Finder of Somatic Fusion Genes in RNA-seq data☆141Updated last year
- A Python-based EGA download client☆93Updated 5 months ago
- Software program for checking sample matching for NGS data☆122Updated 3 months ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆84Updated last year
- a Medical Genetics Sequence Analysis Pipeline☆69Updated this week
- ☆81Updated 5 years ago
- Annotation and Ranking of Structural Variation☆210Updated 2 weeks ago
- ☆174Updated last year
- GWAS Pipeline for H3Africa☆104Updated this week
- Personal Cancer Genome Reporter (PCGR)☆251Updated last month
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆122Updated 4 years ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆138Updated this week
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆71Updated 3 months ago
- dbSNP☆121Updated 2 months ago
- MOsaic CHromosomal Alterations (MoChA) caller☆79Updated last month
- Extensible specification for representing and uniquely identifying biological sequence variation☆80Updated last week
- Precision HLA typing from next-generation sequencing data☆182Updated 6 months ago
- GATK RNA-Seq Variant Calling in Nextflow☆131Updated last year
- The nimble & robust variant annotator☆170Updated 4 months ago
- Workflows for germline short variant discovery with GATK4☆133Updated 3 years ago
- A structural variation pipeline for short-read sequencing☆169Updated this week
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆129Updated last month
- VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.☆92Updated 4 months ago
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆106Updated 5 years ago